Quality Control Analyst – Raw Materials & Finished Products

Rosemont Pharmaceuticals; Leeds; On-site; GBP 26,000 - 38,000; Full time

Benefits offered by this job

Healthcare Cash Plan

Pension contribution (3% employee / 5%

26 Days Annual Leave + Bank Holidays

Hybrid working hours

On-Site Parking

Rewards Platform

Job summary

Rosemont Pharmaceuticals seeks an Assistant/Associate Analyst in Quality Control at our Leeds site. You will perform finished-product, raw-material and packaging testing, using validated methods and HPLC, while ensuring GMP compliance and accurate documentation.

The role spans routine testing, investigations, calibration, and procedure updates in a regulated lab. The successful candidate will have a scientific degree or equivalent A-levels with GMP experience, strong attention to detail, and

Qualifications

• Bachelor’s degree or two A levels with GMP analytical experience.
• Associate Analyst: 2+ years’ relevant work experience, or >3 years GMP analysis with A levels/T Level.
• Assistant Analyst: A levels/T Level with >1 year GMP analytical experience.
• GMP, SOPs and Quality Management Systems understanding.
• Strong attention to detail and accurate documentation.

Responsibilities

• Perform physical and analytical testing of finished products, raw materials, and components.
• Conduct analytical testing using HPLC and related techniques.
• Carry out chemistry, microbiology and preservative efficacy testing per pharmacopoeial monographs.
• Document results in accordance with data-documentation practices.
• Review data from internal and contract laboratories for accuracy and regulatory compliance.
• Identify and report out-of-specification, out-of-trend, or aberrant results.
• Support investigations and root-cause analyses.
• Calibrate, maintain, and qualify laboratory instrumentation.
• Prepare and revise QC procedures, work instructions and reports.
• Support stability studies, risk assessments and environmental monitoring.

Skills

Quality control

GMP knowledge

Analytical testing

HPLC

Documentation

Education

Bachelor’s degree in a scientific discipline

Two A levels or a T Level with GMP experience

Tools

HPLC

Laboratory instrumentation

Job description

Rosemont Pharmaceuticals seeks an Assistant/Associate Analyst in Quality Control at our Leeds site. You will perform finished-product, raw-material and packaging testing, using validated methods and HPLC, while ensuring GMP compliance and accurate documentation.

The role spans routine testing, investigations, calibration, and procedure updates in a regulated lab. The successful candidate will have a scientific degree or equivalent A-levels with GMP experience, strong attention to detail, and